A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546933



Internal ID20920144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61681779..61688902hg38UCSC Ensembl
chr20:60256835..60263958hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387124
hg197124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068305
Samples
Known GenesCDH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546933
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer